Chain415: Congenital Slow Channel Myasthenic Syndrome
This is a rare disease.
Example use A
Rare disease screening of newborns or adults thinking of having children. Could also be used as part of a comprehensive analysis of a person's genes.
Developer
Dr. Colby
Genetic info
Genes | Genetic variants |
---|---|
CHRNB1 | chr17:7357648,chr17:7357660 |
CHRNE | chr17:4804366,chr17:4805305,chr17:4804140 |
CHRNA1 | chr2:175618970 |